Quality Engineer – 2nd Shift, Vascular Devices

Regulatory Jobs

Temecula (CA)

Vor Ort

USD 61.000 - 123.000

Vollzeit

Vor 6 Tagen
Sei unter den ersten Bewerbenden
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Benefits dieser Stelle

Medical coverage
Retirement plan
Tuition reimbursement

Zusammenfassung

Abbott in Temecula, CA is seeking a Quality Engineer for the 2nd shift in the Vascular division, an onsite role. You will provide process and quality engineering support to manufacturing and product development to ensure the highest quality products reach customers.

The role emphasizes CAPA, data analysis, risk management, and adherence to quality systems, with expectations to lead process improvements and collaborate across teams within a regulated medical devices environment.

Qualifikationen

  • Bachelor's degree in a related field with 2–5 years of experience.
  • CAPA experience, data analysis and risk management skills.
  • Familiarity with medical devices quality systems.

Aufgaben

  • Provide process and quality engineering support to manufacturing to ensure high-quality products.
  • Support product development teams to deliver quality new products.
  • Identify and control manufacturing defects and implement corrective actions.
  • Develop quality plans, specifications, and release criteria with the team.
  • Create risk analyses and FMEAs as part of quality improvement.
  • Lead process monitoring and data analysis to reduce variation and defects.
  • Contribute to quality tools and training materials for the site.

Kenntnisse

CAPA
Data Analysis
Risk Management
Quality Systems

Ausbildung

Bachelor's degree or Master's in a related field

Jobbeschreibung

Abbott in Temecula, CA is seeking a Quality Engineer for the 2nd shift in the Vascular division, an onsite role. You will provide process and quality engineering support to manufacturing and product development to ensure the highest quality products reach customers.

The role emphasizes CAPA, data analysis, risk management, and adherence to quality systems, with expectations to lead process improvements and collaborate across teams within a regulated medical devices environment.

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